Bepridil inhibition of sodium current in rat hippocampal CA1 neurons

被引:0
|
作者
Hu, HJ
Yang, DM
Dai, DZ [1 ]
Wu, CH
Zhou, PA
机构
[1] China Pharmaceut Univ, Div Pharmaceut Res, Nanjing 210009, Peoples R China
[2] China Pharmaceut Univ, Dept Pharmacol Chinese Materia Med, Nanjing 210009, Peoples R China
[3] Natl Lab Biomembrane & Membrance Biotechnol, Beijing 100871, Peoples R China
来源
ACTA PHARMACOLOGICA SINICA | 1999年 / 20卷 / 09期
关键词
hippocampus; patch-clamp techniques; bepridil; sodium channels; electrophysiology;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
AIM: To study the effects of bepridil on sodium current in rat hippocampal neurons. METHODS: All, experiments were performed on acutely isolated hippocampal pyramidal neurons by means of whole-cell patch-clamp techniques. Recording media contained ion channel blockers to allow the selective activation of voltage-dependent sodium currents. RESULTS: Bepridil reduced the amplitudes of sodium current in time- and concentration-dependent manners. The half-blocking time was about 10 min in bepridil 10 mu mol L-1, and IC50 was 2.6 (2.3 - 2.9) mu mol. L-l Bepridil 10 mu mol.L-1 shifted the maximal activation of sodium current from - 50 mV to - 40 mV, and the characteristic voltage of inactivation from - 71 mV to -89 mV without changing the slope factor. CONCLUSION: Bepridil blocked voltage-dependent sodium current of hippocampal CA1 neurons and might have therapeutic actions for ischemia-induced brain damage.
引用
收藏
页码:819 / 823
页数:5
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